Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
24599 | 257 | 20.0 | 70% |
Classes in level above (level 2) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
409 | 16055 | WOLF HIRSCHHORN SYNDROME//HOLOPROSENCEPHALY//ANNALES DE GENETIQUE |
Terms with highest relevance score |
Rank | Term | Type of term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|---|
1 | PALLISTER KILLIAN SYNDROME | Author keyword | 191 | 95% | 24% | 62 |
2 | TETRASOMY 12P | Author keyword | 60 | 100% | 8% | 20 |
3 | TRISOMY 12P | Author keyword | 27 | 92% | 4% | 11 |
4 | MOSAIC TETRASOMY 12P | Author keyword | 15 | 88% | 3% | 7 |
5 | ISOCHROMOSOME 12P | Author keyword | 12 | 44% | 8% | 21 |
6 | PALLISTER KILLIAN | Author keyword | 8 | 100% | 2% | 5 |
7 | PALLISTER KILLIAN SYNDROME PKS | Author keyword | 8 | 100% | 2% | 5 |
8 | TRISOMY 12P SYNDROME | Author keyword | 6 | 80% | 2% | 4 |
9 | 12P TETRASOMY | Author keyword | 6 | 100% | 2% | 4 |
10 | 12P DUPLICATION | Author keyword | 4 | 75% | 1% | 3 |
Web of Science journal categories |
Author Key Words |
Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
LCSH search | Wikipedia search |
---|---|---|---|---|---|---|---|
1 | PALLISTER KILLIAN SYNDROME | 191 | 95% | 24% | 62 | Search PALLISTER+KILLIAN+SYNDROME | Search PALLISTER+KILLIAN+SYNDROME |
2 | TETRASOMY 12P | 60 | 100% | 8% | 20 | Search TETRASOMY+12P | Search TETRASOMY+12P |
3 | TRISOMY 12P | 27 | 92% | 4% | 11 | Search TRISOMY+12P | Search TRISOMY+12P |
4 | MOSAIC TETRASOMY 12P | 15 | 88% | 3% | 7 | Search MOSAIC+TETRASOMY+12P | Search MOSAIC+TETRASOMY+12P |
5 | ISOCHROMOSOME 12P | 12 | 44% | 8% | 21 | Search ISOCHROMOSOME+12P | Search ISOCHROMOSOME+12P |
6 | PALLISTER KILLIAN | 8 | 100% | 2% | 5 | Search PALLISTER+KILLIAN | Search PALLISTER+KILLIAN |
7 | PALLISTER KILLIAN SYNDROME PKS | 8 | 100% | 2% | 5 | Search PALLISTER+KILLIAN+SYNDROME+PKS | Search PALLISTER+KILLIAN+SYNDROME+PKS |
8 | TRISOMY 12P SYNDROME | 6 | 80% | 2% | 4 | Search TRISOMY+12P+SYNDROME | Search TRISOMY+12P+SYNDROME |
9 | 12P TETRASOMY | 6 | 100% | 2% | 4 | Search 12P+TETRASOMY | Search 12P+TETRASOMY |
10 | 12P DUPLICATION | 4 | 75% | 1% | 3 | Search 12P+DUPLICATION | Search 12P+DUPLICATION |
Key Words Plus |
Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|
1 | MOSAIC TETRASOMY 12P | 79 | 94% | 11% | 29 |
2 | TETRASOMY 12P | 79 | 94% | 11% | 29 |
3 | ISOCHROMOSOME 12P | 24 | 60% | 10% | 26 |
4 | EXTRA ISOCHROMOSOMES | 19 | 80% | 5% | 12 |
5 | TRISOMY 12P | 13 | 67% | 5% | 12 |
6 | I12P SYNDROME | 11 | 100% | 2% | 6 |
7 | 12P | 10 | 39% | 8% | 21 |
8 | I12P | 9 | 30% | 10% | 25 |
9 | DUPLICATION 12Q | 9 | 83% | 2% | 5 |
10 | LACTICO DEHYDROGENASE B | 6 | 80% | 2% | 4 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references |
% act. ref. to same field |
---|---|---|---|---|
Subtelomeric Deletion of 12p: Description of a Third Case and Review | 2010 | 10 | 13 | 46% |
Parental origin of the isochromosome 12p in Pallister-Killian syndrome: Molecular analysis of one patient and review of the reported cases | 1999 | 26 | 14 | 86% |
Subtle trisomy 12q24.3 and subtle monosomy 22q13.3: Three new cases and review | 2003 | 4 | 25 | 28% |
GENETIC RISKS FOR FAMILIAL RECIPROCAL TRANSLOCATIONS WITH SPECIAL EMPHASIS ON THOSE LEADING TO 9P, 10P AND 12P TRISOMIES | 1982 | 33 | 4 | 50% |
Address terms |
Rank | Address term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|
1 | CHILD PSYCHOPATHOL UNIT NEUROPSYCHOL DEV DISORDER | 1 | 50% | 0.4% | 1 |
2 | CLIN GENET POST PROGRAM PATHOL | 1 | 50% | 0.4% | 1 |
3 | MED GENET EXPT MED PATHOL | 1 | 50% | 0.4% | 1 |
4 | PEDIAT NEONATAL PATHOL UNIT | 1 | 50% | 0.4% | 1 |
5 | PHONIATR PEDAUD | 1 | 50% | 0.4% | 1 |
6 | SC NEUROPSICHIATRIA INFANTILE | 1 | 50% | 0.4% | 1 |
7 | SERV GYNECOL 1 | 1 | 50% | 0.4% | 1 |
8 | SIGNATURE GENOM | 1 | 50% | 0.4% | 1 |
9 | UFR MED REIMS | 1 | 50% | 0.4% | 1 |
10 | UOSD MED GENET | 1 | 50% | 0.4% | 1 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000221945 | CAT EYE SYNDROME//SUPERNUMERARY MARKER CHROMOSOMES//SMALL SUPERNUMERARY MARKER CHROMOSOME |
2 | 0.0000196809 | TRISOMY 9P//TETRASOMY 9P//PARTIAL TRISOMY 7P |
3 | 0.0000164840 | CONFINED PLACENTAL MOSAICISM//UNIPARENTAL DISOMY//TRISOMY 9 |
4 | 0.0000149526 | TRISOMY 10Q//MONOSOMY 10Q//10P TRISOMY |
5 | 0.0000135581 | CRI DU CHAT SYNDROME//CRI DU CHAT//3P DELETION SYNDROME |
6 | 0.0000122573 | RING CHROMOSOME 21//MONOSOMY 21//RING CHROMOSOME 15 |
7 | 0.0000122390 | SUBTELOMERIC REARRANGEMENTS//IDIOPATHIC MENTAL RETARDATION//MBD5 |
8 | 0.0000116922 | PITT HOPKINS SYNDROME//18Q DELETION SYNDROME//18Q SYNDROME |
9 | 0.0000105698 | WOLF HIRSCHHORN SYNDROME//4P DELETION//PITT ROGERS DANKS SYNDROME |
10 | 0.0000105125 | COMPLEX CHROMOSOMAL REARRANGEMENT//COMPLEX CHROMOSOME REARRANGEMENT CCR//COMPLEX CHROMOSOMAL REARRANGEMENTS |